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The results of the above studies suggest that genetic testing and phenotyping should be ordered in patients with elevated Lp(a) levels, which could serve as an additional tool to assess CVD risk, to personalise and select the best available therapy (statins, niacin, PCSK9 inhibitors) [142, 143]

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For some populations, the availability of these interventions may be restricted by the high expense of genetic testing and cutting-edge technologies combined with inequalities in healthcare access (140)

However, some notes about our study must be highlighted

A recent meta-analysis conducted by Patel et al